April M. Hacker

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion

Sulagna C. Saitta, Stacy E. Harris, Ann P. Gaeth et al. · Human Molecular Genetics · 2003 · 147 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays

Alexander E. Urban, Jan O. Korbel, Rebecca R. Selzer et al. · Proceedings of the National Academy of Sciences · 2006 · 141 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q

Jacob Vorstman, G R Jalali, Eric Rappaport et al. · Human Mutation · 2006 · 140 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Low copy repeats mediate distal chromosome 22q11.2 deletions: Sequence analysis predicts breakpoint mechanisms

Tamim H. Shaikh, Ronald J. O’Connor, Mary Ella Pierpont et al. · Genome Research · 2007 · 125 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

A Palindrome-Mediated Recurrent Translocation with 3:1 Meiotic Nondisjunction: The t(8;22)(q24.13;q11.21)

Molly B. Sheridan, Takema Kato, Chad Haldeman‐Englert et al. · The American Journal of Human Genetics · 2010 · 118 citations · Full text

Medicine, Genetics, Molecular Genetics +7